The total synthesis of the new sesquiterpenoid (±)-fulvanin 1/sollasin a

Article abstract of DOI:10.1016/0040-4039(95)00321-3

The reaction of 2,3-dimethylcyclohexan-1-one (2) with the functionalized allylic bromide 3 produced regio- and stereoselectively a precursor (4) of the new sesquiterpenoid sollasin a/fulvanin 1 (1). Functional group transformations then completed the synt